SCHEMBL4524759

SCHEMBL4524759

Fc1cc(CCl)ccc1Cl

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 1/20 0.42
MAPK1 P28482 1/20 0.42
PNMT P11086 1/20 0.40
TAAR1 Q96RJ0 1/20 0.40
GRM2 Q14416 1/20 0.39
IDO1 P14902 2/20 0.38
SLC6A3 Q01959 3/20 0.37
TTR P02766 2/20 0.37
PPARG P37231 1/20 0.36
PPARA Q07869 1/20 0.36
RAPGEF4 Q8WZA2 1/20 0.35
SLC6A4 P31645 2/20 0.34
SLC6A2 P23975 1/20 0.34
SIGMAR1 Q99720 1/20 0.33
CYP1A2 P05177 1/20 0.33
CYP2D6 P10635 1/20 0.33
CYP2C9 P11712 1/20 0.33
CYP2C19 P33261 1/20 0.33
GPR84 Q9NQS5 1/20 0.33
HRH3 Q9Y5N1 1/20 0.33

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL31634179 1.00 MAPT (0.42) MAPTMAPK1PNMTTAAR1GRM2
SCHEMBL29042669 0.82 PNMT (0.47) MAPTMAPK1PNMTTAAR1GRM2
SCHEMBL1503218 0.81 PIK3CA (0.45) MAPTPNMTTAAR1IDO1SLC6A3
SCHEMBL29489387 0.80 HTT (0.45) TTR
SCHEMBL1503157 0.80 HTT (0.45) TTR
SCHEMBL20245287 0.79 MAPT (0.41) MAPTMAPK1PNMTTAAR1GRM2
SCHEMBL3746892 0.79 MAPT (0.45) MAPTMAPK1PNMTTAAR1GRM2
SCHEMBL2092845 0.79 MAPT (0.41) MAPTMAPK1PNMTTAAR1GRM2
SCHEMBL2092848 0.79 MAPT (0.45) MAPTMAPK1PNMTTAAR1GRM2
SCHEMBL257064 0.79 TRPA1 (0.41) MAPTMAPK1PNMTTAAR1GRM2

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 24 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11332459-B2 Benzimidazole derivatives and their uses TEIJIN PHARMA LIMITED (JP) 2022-05-17 US disclosed
US-20200308145-A1 BENZIMIDAZOLE DERIVATIVES AND THEIR USES AMGEN INC. (US) 2020-10-01 US disclosed
EP-2805954-B1 7-SUBSTITUTED HANFANGICHIN B DERIVATIVE, AND PREPARATION METHOD AND USE THEREOF HANGZHOU BENSHENG PHARMACEUTICAL CO LTD (CN) 2019-06-19 EP disclosed
EP-2805954-B1 7-SUBSTITUTED HANFANGICHIN B DERIVATIVE, AND PREPARATION METHOD AND USE THEREOF HANGZHOU BENSHENG PHARMACEUTICAL CO LTD (CN) 2019-06-19 EP disclosed
US-9328122-B2 7-substituted Hanfangichin B derivative, and preparation method and use thereof HANGZHOU BENSHENG PHARMACEUTICALS CO., LTD. (CN) 2016-05-03 US disclosed
US-9328122-B2 7-substituted Hanfangichin B derivative, and preparation method and use thereof HANGZHOU BENSHENG PHARMACEUTICALS CO., LTD. (CN) 2016-05-03 US disclosed
US-9328122-B2 7-substituted Hanfangichin B derivative, and preparation method and use thereof HANGZHOU BENSHENG PHARMACEUTICALS CO., LTD. (CN) 2016-05-03 US disclosed
US-20140357647-A1 7-SUBSTITUTED HANFANGICHIN B DERIVATIVE, AND PREPARATION METHOD AND USE THEREOF HANGZHOU BENSHENG PHARMACEUTICAL CO., LTD. (CN) 2014-12-04 US disclosed
US-20140357647-A1 7-SUBSTITUTED HANFANGICHIN B DERIVATIVE, AND PREPARATION METHOD AND USE THEREOF HANGZHOU BENSHENG PHARMACEUTICAL CO., LTD. (CN) 2014-12-04 US disclosed
US-20140357647-A1 7-SUBSTITUTED HANFANGICHIN B DERIVATIVE, AND PREPARATION METHOD AND USE THEREOF HANGZHOU BENSHENG PHARMACEUTICAL CO., LTD. (CN) 2014-12-04 US disclosed
EP-1984349-A1 PIPERIDINE DERIVATIVES AS CXCR3 RECEPTOR ANTAGONISTS Janssen Pharmaceutica, N.V. (BE) 2008-10-29 EP disclosed
CN-100374440-C Spirosubstituted piperidines as selective melanin concentrating hormone receptor antagonists for the treatment of obesity SCHERING CORP (US) 2008-03-12 CN disclosed
WO-2007090826-A1 PIPERIDINE DERIVATIVES AS CXCR3 RECEPTOR ANTAGONISTS JANSSEN PHARMACEUTICA N.V. (BE) 2007-08-16 WO disclosed
US-20060063782-A1 3-Hetero arylmethoxy ! pyridines and their analogues as p38 map kinase inhibitors ASTEX THERAPEUTICS LIMITED (GB) 2006-03-23 US disclosed
CN-1665812-A Spirosubstituted piperidines as selective melanin concentrating hormone receptor antagonists for the treatment of obesity SCHERING CORP (US) 2005-09-07 CN disclosed
EP-1545523-A1 3-&-grave;(HETERO) ARYLMETHOXY ! PYRIDINES AND THEIR ANALOGUES ASP38 MAP KINASE INHIBITORS Astex Technology Limited (GB) 2005-06-29 EP disclosed
WO-2005002673-A1 RAF KINASE INHIBITORS ASTEX THERAPEUTICS LIMITED (GB) 2005-01-13 WO disclosed
WO-2004004720-A1 3-`(HETERO) ARYLMETHOXY ! PYRIDINES AND THEIR ANALOGUES AS P38 MAP KINASE INHIBITORS ASTEX TECHNOLOGY LIMITED (GB) 2004-01-15 WO disclosed
CN-1099030-A Biocidal compounds SHELL INT RESEARCH (NL) 1995-02-22 CN disclosed
EP-0623601-A1 N-(3-Fluorobenzyl)heterocyclic derivatives and their use as pesticides SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) 1994-11-09 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20060063782-A1 3-Hetero arylmethoxy ! pyridines and their analogues as p38 map kinase inhibitors MAPK1, MAPK3, MAPK10 MAPT 2630/4885MAPK1 1/4885PNMT 1640/4885
US-20200308145-A1 BENZIMIDAZOLE DERIVATIVES AND THEIR USES TRPC6, TRPV6, TRPM6 MAPT 3674/4885MAPK1 2222/4885PNMT 3338/4885
US-20140357647-A1 7-SUBSTITUTED HANFANGICHIN B DERIVATIVE, AND PREPARATION METHOD AND USE THEREOF UGT2B7, CYP3A7, UGT1A7 MAPT 4497/4885MAPK1 1302/4885PNMT 688/4885
US-11332459-B2 Benzimidazole derivatives and their uses TRPC6, TRPV6, TRPM6 MAPT 3674/4885MAPK1 2222/4885PNMT 3338/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.